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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1863079Generated: October 31, 2026

Ammonia → HCID 20393354, compound

https://huagongshe.com/reaction/1863079

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAmmoniaHCID 222—
ReactantSodium cyanoborohydrideHCID 5003444—
ReactantHCID 20393335HCID 20393335—
ProductHCID 20393354HCID 20393354—

Reaction Steps

In accordance with the procedure described in Example 3, 16.0 g. of o-benzoyl-p-chlorophenylglyoxylic acid [2-(diethylamino)ethyl]methylamide are reacted with 4.1 g. of ammonia and 1.6 g. of sodium cyanoborohydride. The ether extract containing the free base is concentrated to about 300 ml. and treated with ethereal hydrochloric acid. The precipitated hydrochloride is recrystallized from ethanol, and there is obtained 5-chloro-3-phenylisoindole-1-carboxylic acid [2-(diethylamino)ethyl]methylamide hydrochloride in the form of felt-like greenish crystals having a melting point of 208°-210° C. (decomposition).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04167632
Source datasetuspto-grants-1979_09
ORD IDord-729e83bffcb14033ab91796ea797da8f
Source noteuspto-grants-1979_09